Details for FSHR:c.884C>T, p.Ser295Phe

CHROMOSOME 2
GENOMIC COORDINATES
hg19hg38
4919107648963937
VARIANT EFFECT None
ANNOTATION FLAG None
GENE FSHR
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_000145.4
CDNA CHANGE c.884C>T
PROTEIN CHANGE p.Ser295Phe
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging3.811491Polymorphism
DBSNP ID NA
1 combination linked to FSHR:c.884C>T, p.Ser295Phe OLI1722
1 disease linked to FSHR:c.884C>T, p.Ser295Phe Primary ovarian failure

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